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Associate Supply Chain Reverse Logistics and Ops support

LocationBreda, Netherlands
Business SectorBiotechnology
Contact nameDaria Finikova
Contact email
Job ref26093
Publishedabout 16 hours ago
Accountabilities?
  • Support daily operations related to reverse logistics, tracking and tracing, serialization, and distribution complaints throughout the EMEA region.
  • Ensure compliance in managing third-party distribution complaints and returns while meeting the established key performance indicators (KPIs).
  • Ensure compliance with SOX and GDP regulations.
  • Attention to detail and a quality mindset in all activities determine the root causes of problems with limited scope and complexity.
Responsibilities???
  • Monitors and coordinates the return of Finished Drug Products (FDP) to Amgen Sites (ABR/ADL), CMO or Amgen Warehouses or LSP locations. Including re-calls.
  • Log, investigate, and follow up on low-risk distribution complaints by coordinating with relevant stakeholders. Ensure that all records are accurately initiated and concluded within the designated timelines and in compliance with regulatory requirements.
  • Support tracking and tracing activities for shipments under the Global distribution Hub, providing daily oversight and collaborating with the business process owner.
  • Perform daily analysis of alerts received from the National Medicines Verification Organization (NMVO) and own the monthly and quarterly EU FMD Alert trend reporting process
  • Supports team and business with continuous improvements
  • Represent the team during Stakeholder management meetings
  • Participates in ABR internal and external audits as needed.
  • Other duties may be assigned to you as required.
Outputs
  • Ensures Amgen's policies and procedures are followed to ensure complete compliance.
  • Continuously seek opportunities for improvement and generate innovative ideas to enhance the quality of our services.
  • Supports the achievement of our departmental and global goals and initiatives
Minimum Requirements
  • Master’s or bachelor’s degree with two years of Supply Chain experience in a GMP and GDP-regulated industry.
  • Ability to multitask and work with a diverse, international group.
  • Advanced communication skills
  • Computer skills and ERP experience
  • Experience with issue handling in a logistic environment
  • Problem-solving skills
  • Proactive self-starter who can manage workload and prioritise tasks efficiently.
  • Proficiency in the English language is required for both written and oral communication.
  • Ensure quality.
?Preferred Requirements
  • Preferably 3+ yrs' relevant experience in the biotech/pharma industry & strong understanding of supply chain, order-to-invoicing & international trade.
  • Understanding of GMP regulations, GDP guidelines, and SOX regulations.
  • Lean Six Sigma certification is a plus.
Interested? Send your CV to Daria at d.finikova@panda-int.com or call +31202044502 for more info.